A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535366



Internal ID20908727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38859787..38882916hg38UCSC Ensembl
chr19:39350427..39373556hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3823130
hg1923130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198111
Samples
Known GenesRINL, SIRT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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